Associated Papers
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
Khan H et al.
Scientific Reports, 2024
39271758 (PubMed )
Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › HPK7_het
Loss-of-function OGFRL1 variants identified in autosomal recessive cherubism families.
Kittaka M et al.
Jbmr Plus, 2024
38699440 (PubMed )
Supplement: supplementary_table_1_new_ziae050.xlsx › Supplementary_Table_1
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